bilirubin - very light-sensitive chemical and is rapidly destroyed when exposed to light.
hyperbilirubinemia - increased serum bilirubin
hyperbilirubinemia - may be caused by the presence of hemolytic disease of the newborn or it may simply occur because the liver of newborns is often not developed enough
Bilirubin test results - are critical to infant survival and mental health
The decision to perform an exchange transfusion is based on the bilirubin levels and the newborn’s age and condition.
Phlebotomy technique is critical to the determination of accurate bilirubin results, and samples must be collected quickly and protected from excess light during and after the collection.
Infants who appear jaundiced are frequently placed under an ultraviolet light (UV) to lower the level of circulating bilirubin.
UV light must be turned off during sample collection
Amber-colored microcollection tubes are available for collecting bilirubin, or if multiple capillary pipettes are used, the filled tubes should be shielded from light.
Hemolysis must be avoided; it will falsely lower bilirubin results in some procedures and must be corrected for in others.
samples must be collected at the specified time so that the rate of bilirubin increase can be determined
When collecting samples for neonatal bilirubin tests, turn off the ultraviolet light during collection unless it is a newer model that is strapped directly to the infant.
Bilirubin levels may decrease as much as 50% in a blood sample that has been exposed to light for 2 hours
Newborn screening - the testing of newborn babies for genetic, metabolic, hormonal, and functional disorders that can cause physical disabilities, mental retardation, or even death, if not detected and treated early.
Screening of newborns for 50 inherited metabolic disorders can currently be performed from blood collected by heelstick and placed on specially designed filter paper
Many of these disorders can be prevented by early changes in the newborn’s diet or early administration of a missing hormone. Examples of the common disorders phenylketonuria (PKU), congenital hypothyroidism, and galactosemia
Newborn screening tests are performed on blood collected by dermal puncture, except for the hearing test.
Ideally blood is collected between 24 and 72 hours after birth, before the baby is released from the hospital.
It is recommended that the newborn screening samples should be collected separately, after prewarming and puncturing a second site when additional blood tests are requested.
The phlebotomist must be careful not to touch or contaminate the area inside the circles or to touch the dried blood spots.
phenylketonuria - caused by the lack of the enzyme needed to metabolize the amino acid phenylalanine
phenylketonuria - accumulates and causes problems with brain development and mental retardation
early detection of phenylketonuria is crucial because the damage is irreversible but can be treated with a diet low in phenylketonuria and high in tyrosine
Congenital hypothyroidism - a thyroid hormone deficiency present at birth
congenital hypothyroidism - delays in growth and brain development that produce mental retardation can be avoided by the use of oral doses of thyroid hormone within the first few weeks after birth
Galactosemia - a genetic metabolic disorder caused by the lack of the liver enzyme needed to convert galactose (sugar in milk) into glucose
galactosemia - Galactose accumulates in the blood and can cause liver disease, renal failure, cataracts, blindness, mental retardation, and death.
galactosemia - treatment of this is the elimination of all milk and dairy products from the infant for life.
heelstick - performed in the routine manner, and the first drop of blood is wiped away
To prevent cross-contamination, samples should not be hung to dry or stacked during or after the drying process.
When dry, the sample is placed in a special envelope and sent to the appropriate laboratory for testing.
Be sure that all required patient information is filled out on the neonatal screening test form.
Uneven or incomplete saturation of filter paper circles because of layering from multidrop application will yield an unacceptable sample for testing.
Specific state mandates for newborn screening can be found at the U.S. National Newborn Screening and Genetics Resource Center website
Blood spots must be thoroughly dry before the attached fold-over flap is closed over the spots.
Arterial blood - the preferred sample for blood gases (oxygen and carbon dioxide content) and pH levels in adults
Performing deep arterial punctures in newborns and young children is usually not recommended
blood gases - are performed on capillary blood
Blood is collected from the plantar area of the heel or big toe and the palmar area of the fingers
capillary blood is actually a mixture of venous and arterial blood, with a higher concentration of arterial blood.